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8omg

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'''Unreleased structure'''
 
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The entry 8omg is ON HOLD
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==Crystal structure of mKHK (apo)==
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<StructureSection load='8omg' size='340' side='right'caption='[[8omg]], [[Resolution|resolution]] 1.82&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8omg]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8OMG OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8OMG FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.82&#8491;</td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8omg FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8omg OCA], [https://pdbe.org/8omg PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8omg RCSB], [https://www.ebi.ac.uk/pdbsum/8omg PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8omg ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/KHK_MOUSE KHK_MOUSE] Catalyzes the phosphorylation of the ketose sugar fructose to fructose-1-phosphate.[UniProtKB:P50053]
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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A molecular understanding of the proteins involved in fructose metabolism is essential for controlling the current spread of fructose-related obesity, diabetes and related adverse metabolic states in Western populations. Fructose catabolism starts with the phosphorylation of D-fructose to fructose 1-phosphate by ketohexokinase (KHK). KHK exists in two alternatively spliced isoforms: the hepatic and intestinal isoform KHK-C and the peripheral isoform KHK-A. Here, the structure of apo murine KHK (mKHK), which differs from structures of human KHK in overall conformation, is reported. An isoform-selective ligand, which offers a 50-fold higher potency on mKHK and human KHK-A compared with KHK-C, is further characterized. In mKHK, large-scale conformational changes are observed upon ligand binding. The structures suggest a combined strategy for the design of species- and isoform-selective KHK inhibitors.
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Authors: Ebenhoch, E., Pautsch, P.
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Crystal structures of human and mouse ketohexokinase provide a structural basis for species- and isoform-selective inhibitor design.,Ebenhoch R, Bauer M, Romig H, Gottschling D, Kley JT, Heine N, Weber A, Uphues I, Nar H, Pautsch A Acta Crystallogr D Struct Biol. 2023 Oct 1. doi: 10.1107/S2059798323006137. PMID:37712434<ref>PMID:37712434</ref>
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Description: Crystal structure of mKHK (apo)
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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[[Category: Ebenhoch, E]]
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<div class="pdbe-citations 8omg" style="background-color:#fffaf0;"></div>
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[[Category: Pautsch, P]]
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Large Structures]]
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[[Category: Mus musculus]]
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[[Category: Ebenhoch E]]
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[[Category: Pautsch P]]

Current revision

Crystal structure of mKHK (apo)

PDB ID 8omg

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